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活动性结核病与 HIV 感染者中 HIV 特异性 CD4 和 CD8 T 细胞耗竭有关。

Active Tuberculosis Is Associated with Depletion of HIV-Specific CD4 and CD8 T Cells in People with HIV.

机构信息

Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.

Department of Biomedical Sciences, School of Public Health and Community Development, Maseno University, Kisumu, Kenya.

出版信息

AIDS Res Hum Retroviruses. 2024 Jul;40(7):417-427. doi: 10.1089/AID.2023.0088. Epub 2024 Mar 14.

Abstract

Infection with (Mtb) in people with HIV (PWH) is associated with depletion of Mtb-specific CD4 T cell responses, increased risk of progression to active tuberculosis (TB) disease, and increased immune activation. Although higher HIV viral loads have been reported in Mtb/HIV co-infection, the extent to which Mtb infection and TB disease impact the frequency and phenotype of HIV-specific T cell responses has not been well described. We enrolled a cohort of PWH in Kenya across a spectrum of Mtb infection states, including those with no evidence of Mtb infection, latent Mtb infection (LTBI), and active pulmonary TB disease, and evaluated the frequency, immune activation, and cytotoxicity phenotype of HIV-specific CD4 and CD8 T cell responses in peripheral blood by flow cytometry. We found evidence of depletion of HIV-specific CD4 and CD8 T cells in people with TB, but not with LTBI. Expression of the immune activation markers human leukocyte antigen-DR isotype (HLA-DR) and Ki67 and of the cytotoxic molecules granzyme B and perforin were increased in total CD4 and CD8 T cell populations in individuals with TB, although expression of these markers by HIV-specific CD4 and CD8 T cells did not differ by Mtb infection status. These data suggest that TB is associated with overall increased T cell activation and cytotoxicity and with depletion of HIV-specific CD4 and CD8 T cells, which may contribute to further impairment of T cell-mediated immune control of HIV replication in the setting of TB.

摘要

在人类免疫缺陷病毒(HIV)感染者(PWH)中,感染(Mtb)与 Mtb 特异性 CD4 T 细胞反应的耗竭、进展为活动性结核病(TB)疾病的风险增加以及免疫激活增加有关。尽管已经报道在 Mtb/HIV 共感染中 HIV 病毒载量更高,但 Mtb 感染和 TB 疾病对 HIV 特异性 T 细胞反应的频率和表型的影响程度尚未得到很好的描述。我们在肯尼亚招募了一组 HIV 感染者,涵盖了一系列 Mtb 感染状态,包括没有 Mtb 感染、潜伏性 Mtb 感染(LTBI)和活动性肺结核疾病的感染者,并通过流式细胞术评估了外周血中 HIV 特异性 CD4 和 CD8 T 细胞反应的频率、免疫激活和细胞毒性表型。我们发现 TB 患者的 HIV 特异性 CD4 和 CD8 T 细胞存在耗竭的证据,但 LTBI 患者则没有。在 TB 患者的总 CD4 和 CD8 T 细胞群体中,人类白细胞抗原-DR 同种型(HLA-DR)和 Ki67 的表达以及细胞毒性分子颗粒酶 B 和穿孔素的表达增加,尽管 HIV 特异性 CD4 和 CD8 T 细胞中这些标志物的表达与 Mtb 感染状态无关。这些数据表明,TB 与总 T 细胞激活和细胞毒性增加以及 HIV 特异性 CD4 和 CD8 T 细胞耗竭有关,这可能导致在 TB 背景下进一步损害 T 细胞介导的 HIV 复制的免疫控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b0d/11295841/83a115cf2b0e/aid.2023.0088_figure1.jpg

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